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  • Articles  (25)
  • Elsevier  (12)
  • Wiley-Blackwell  (12)
  • Cell Press  (1)
  • BioMed Central
  • Molecular Diversity Preservation International
  • Public Library of Science
  • 1980-1984  (25)
  • Chemistry and Pharmacology  (19)
  • Biology  (10)
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  • Articles  (25)
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Year
Journal
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 132-147 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction of selected tetramethylpiperidine derivatives with radicals arising from the Norrish-type I cleavage of dibenzyl ketone under oxygen was studied. Product analyses and kinetic studies showed that the investigated sterically hindered piperidine derivatives have a pronounced effect on both the nature and distribution of the products of photolysis of dibenzyl ketone in the presence of oxygen. Observations indicated that the phenylperacetoxyl radical is formed as an intermediate during irradiation and that it interacts with the additives used. Possible mechanisms of the reactions studied are discussed.The observation that oxidation of an isolated double bond by the radicals formed in dibenzyl ketone photolysis under oxygen is strongly inhibited in the presence of the studied sterically hindered amines is discussed in the light of the results presented. The findings are considered in relation to the problem of polymer stabilization.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 2375-2379 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemically and isotopically pure Al35Cl3 and Al37Cl3 are synthesized from Al (s) and HCl (g). The yield is quantitative and no measurable decrease in isotopic content from HCl to AlCl3 takes place.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 65 (1982), S. 1687-1693 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enrichment of the potassium isotopes is achieved by means of the chemical exchange reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ ^{41} {\rm K}^{\rm + } + ^{39} {\rm KL}^{\rm + } \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\longrightarrow\over{\smash{\longleftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} ^{39} {\rm K}^{\rm + } + ^{41} {\rm KL}^{\rm + } $$\end{document} Where L represents a macrocyclic polyether. Dicyclohexyl-18-crown-6 ((cis-syn-cis)-isomer) was investigated. The single stage-separation factor a=1+ε was determined according to the method of Glueckauf from the elution curve and iso-topic assays. One obtains ε-values of 1.18, 0.84. and 0.74 × 10-3(±5×10-5) at -10, 0 and 10° respectively, in favor of the heavy isotope, indicating an enthalpy of isotopic exchange of -13 ± 4 Joule mol-1.The technical feasibility of a pre-enrichment process for 40K starling with basic laboratory data is discussed.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1467-1487 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vinyl Cations, 37. Rearrangement of Cyclic Homopropargyl Sulfonates to Condensed Cyclobutanones and Cyclopropyl KetonesCyclic homopropargyl sulfonates 8 (tosylates, triflates, nonaflates, and damsylates) are prepared and solvolysed. The resulting rearrangement reactions are studied with respect to the properties of the solvents used, leaving groups, the substituent on the triple bond, and with respect to the ring size of the sulfonates 8.
    Notes: Cyclische Homopropargylsulfonate 8 (Tosylate, Triflate, Nonaflate und Damsylate) werden dargestellt und solvolysiert. Die dabei auftretenden Umlagerungsreaktionen werden in Abhängigkeit von den Eigenschaften der verwendeten Lösungsmittel, von der Abgangsgruppe, von den Substituenten an der Dreifachbindung und in Abhängigkeit von der Ringgröße der Sulfonate 8 untersucht.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 2001-2014 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to 15N NMR Spectroscopy, Protonation and Tautomerism in Purines: Purine, 7-and 9-MethylpurineThe 15N NMR spectra of purine (1), 7- and 9-methylpurine (2, 3) have been measured and assigned in various media (NaOH, H2O, 20% H2SO4, 90% H2SO4, DMSO, CF3CO2H, FSO3H). Protonation sites and tautomer ratios are derived from the σ(15N) data. The effect of N-protonation of the geminal 15N,1H spin-spin coupling constants is discussed.
    Notes: Die 15N-NMR-Spektren von Purin (1), 7- und 9-Methylpurin (2, 3) wurden in verschiedenen Medien (NaOH, H2O, 20% H2SO4, 90% H2SO4, DMSO, CF3CO2H, FSO3H) gemessen und zugeordnet. Aus den σ(15N)-Daten werden Protonierungsorte und Tautomerie-Verhältnisse abgeleitet. Der Einfluß der N-Protonierung auf die geminalen 15N, 1H-Spin-Spin-Kopplungskonstanten wird diskutiert.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 103-115 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the thermal reaction between CF3OF and C3F6 have been investigated between 20 and 75°C. It is a homogeneous chain reaction of moderate length where the main product is a mixture of the two isomers 1-C3F7OCF3 (68%) and 2-C3F7OCF3 (32%). Equimolecular amounts of CF3OOF3 and C6F14 are formed in much smaller quantities. Inert gases and the reaction products have no influence on the reaction, whereas only small amounts of oxygen change the course of reaction and larger amounts produce explosions.The rate of reaction can be represented by eq. (I): The following mechanism explains the experimental results: Reaction (5) can be replaced by reactions (5a) and (5b), without changing the result: Reaction (4) is possibly a two-step reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ E_1 = 15.90 \pm 0.45{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = \left( {7.60 \pm 0.68} \right)10^8 {\rm exp}\left( { - 15,900\,\, \pm \,\,450\,\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \cdot s^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ E^ * \, = \,12.30\, \pm \,0.25\,{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k^ * \, = \,\left( {6.11\, \pm \,0342} \right)10^7 \,{\rm exp}\left( { - 12,300\, \pm \,250\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \, \cdot \,{\rm s}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {E^ * \, - \frac{1}{2}E_1 \, = \,4.35\,{\rm kcal}\, = \,E_3 \, - \,\frac{1}{2}E_4 ;} & {E_3 \,} \\ \end{array} 〉 \,4.35\,{\rm kcal} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \nu \,\left( {{\rm chain}\,{\rm length}} \right)\, = \,1 + \,\frac{{k_3 }}{{k_1 ^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} \left( {2k_4 } \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} }}\left( {\frac{{\left| {{\rm CR}_{\rm 3} {\rm OF}} \right|}}{{\left| {{\rm C}_{\rm 3} {\rm F}_{\rm 6} } \right|}}} \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} $$\end{document} For ∣CF3 = ∣C3F6∣, ν20°C = 36.8, ν50°C = 24.0, and ν70°C = 14.2.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 495 (1982), S. 135-147 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Molybdenum Tetrabromide with Tribromonitro Methane. Crystal Structures of PPh4[Mo(NO)2Br3(OH2)] and PPh4[MoOBr4]Molybdenum tetrabromide reacts with tribromonitro methane above 60°C to form a mixture of Mo(NO)2Br2, MoOBr3 and MoO2Br2. A reaction of this mixture with tetraphenylphosphonium bromide in dibromo methane yields the soluble complexes PPh4[Mo(NO)2Br3], PPh4[MoOBr4], and PPh4[MoO2Br3], which can be separated by fractionated crystallization. Aluminum bromide precipitates the pure insoluble compounds Mo(NO)2Br2 and MoOBr3 resp. from the CH2Br2 solution. Single crystals of the dinitrosyltribromo molybdate were obtained in the form of its monohydrate PPh4[Mo(NO)2Br3(OH2)]. The crystal structure was determined by aid of X-ray diffraction data (2925 observed, independent reflexions, R = 4.2%). PPh4[Mo(NO)2Br3(OH2)] crystallizes tri-clinic in the space group P1 with two formula units per unit cell (a = 1048, b = 1106, c = 1276pm; α = 69.7°, β = 83.6°, γ = 81.2°). The structure consists of PPh4⊕ cations and [MO(NO)2Br3,(OH2)]⊖ anions, in which the NO ligands are cis-positioned and linear . The H2O molecule is situated in trans position to a NO group.PPh4[MoOBr4]. according to the X-ray diffraction measurements (616 independent observed reflexions, R = 5.6%) crystallizes in the tetragonal space group P4/n with two formula units per unit cell (a = b = 1289 pm, c = 783 pm, α = β = γ = 90°).The structure consists of PPh4⊖ cations and [MoOBr4]⊖ anions of the symmetry C4v with the terminal oxo ligand in axial position. The Mo=0 bond (173 pm) corresponds to a double bond. It is significantly longer than in the monohydrate, where it is 163 pm.All compounds are characterized by i.r. spectroscopy.
    Notes: Molybdäntetrabromid reagiert mit Tribromnitromethan oberhalb 60°C zu einem Gemisch von Mo(NO)2Br2, MoOBr3 und MoO2Br2. Durch Umsetzung mit Tetraphenylphosphoniumbromid in Dibrommethan werden daraus die löslichen Komplexe PPh4[Mo(NO)2Br3], PPh4[MoOBr4] und PPh4[MoO2Br3] gebildet, die sich durch fraktionierte Kristallisation voneinander trennen lassen. Mit Aluminiumbromid lassen sich aus den Bromokomplexen in CH2Br2 die schwerlöslichen Verbindungen Mo(NO)2Br2 bzw. MoOBr3 in reiner Form fällen. Das Dinitrosyltribromomolybdat ließ sich als Monohydrat PPh4[Mo(NO)2Br3(OH2)] in Form von Einkristallen erhalten. Die Kristallstruktur wurde mit Hilfe von Röntgenbeugungsdaten ermittelt (2 925 beobachtete, unabhängige Reflexe, R = 4,2%). PPh4[Mo(NO)2Br3(OH)2] kristallisiert in der triklinen Raumgruppe P1 mit zwei Formeleinheiten pro Elementarzelle (a = 1 048, b = 1 106, c = 1 276 pm; α = 69,7°, β = 83,6°, γ = 81,2°). Die Struktur besteht aus PPh4⊕-Kationen und [Mo(NO)2Br3(OH2)]⊖-Anionen, in denen die NO-Liganden in gestreckter Anordnung cis-ständig koordiniert sind. Das H2O-Molekül befindet sich in trans-Position zu einer NO-Gruppe.PPh4[MoOBr4] kristallisiert nach der Röntgenstrukturuntersuchung (616 unabhängige, beobachtete Reflexe, R = 5,6%) in der tetragonalen Raumgruppe P4/n mit zwei Formeleinheiten pro Elementarzelle (a = b = 1 289 pm, c = 783 pm, α = β = γ = 90°).Die Struktur besteht aus PPh4⊕-Kationen und [MoOBr4]⊖-Anionen der Symmetrie C4V mit dem terminalen Oxoliganden in der Achsialposition. Die MoO-Bindungslänge entspricht mit 173 pm etwa einer Doppelbindung. Sie ist deutlich länger als im Monohydrat [MoOBr4(OH2)]⊖, wo sie 163 pm beträgt.Alle Präparate werden IR-spektroskopisch charakterisiert.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 79-85 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Dimethyl Sulfoxide with Molybdenum Tetrabromide and Molybdenum Dibromide Dinitrosyl. Crystal Structure of [MoBr2(NO)2(OSMe2)2]In the cold molybdenum tetrabromide reacts with an equivalent amount of dimethyl sulfoxide forming the solvate [MoBr4(OSMe2)2]; excess dimethyl sulfoxide yields [MoO2Br2(OSMe2)2] which is also obtained by other methods. Molybdenum dibromidedinitrosyl forms the solvate [MoBr2(NO)2(OSMe2)2] in the reaction with dimethyl sulfoxide. According to the i.r. spectra all complexes display O-coordination of the OSMe2 molecules. [MoBr2(NO)2(OSMe2)2] crystallizes monoclinic in the space group P21/c with four formula units per unit cell. The cell dimensions are a = 1236, b = 892, c = 1305 pm, β = 95.2°. 1662 independent observed reflexions were used for refinement; R = 3.8%. The molybdenum atoms are six-coordinated, the O atoms of the dimethyl sulfoxide molecules are in trans-position to the nitrosyl ligands, which form linear groups Mo—N—O.
    Notes: Molybdäntetrabromid reagiert mit der äquivalenten Menge Dimethylsulfoxid unter Kühlung zu dem Solvat [MoBr4(OSMe2)2], mit überschüssigem Dimethylsulfoxid entsteht das auch auf anderem Wege zugängliche [MoO2Br2(OSMe2)2]. Molybdändibromiddinitrosyl bildet mit Dimethylsulfoxid das Solvat [MoBr2(NO)2(OSMe2)2]. Nach den IR-Spektren liegen bei allen Komplexen O-Koordination der OSMe2-Moleküle vor. [MoBr2(NO)2(OSMe2)2] kristallisiert monoklin in der Raumgruppe P21/c mit vier Formeleinheiten pro Elementarzelle. Die Gitterabmessungen sind a = 1236, b = 892, c = 1305 pm, β = 95,2° 1662 unabhängige beobachtete Reflexe, R = 3,8%. Das Molybdän ist sechsfach koordiniert, die O-Atome der Dimethylsulfoxidmoleküle befinden sich in trans-Position zu den in gestreckter Bindung koordinierten cis-ständigen Nitrosylgruppen.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 2 (1984), S. 26-32 
    ISSN: 0263-6484
    Keywords: Hormones ; gonadotropins ; Leydig cells ; perfusion ; steroid hydroxylase ; steroid oxidoreductase ; testis ; testosterone ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Production of testosterone by highly purified Leydig cells prepared from rat and mouse testes is compared. Testosterone formation is improved to a higher degree in rat (2.7-fold) than in mouse (1.7-fold) cells by callagenase treatment of the testis compared with mechanical isolation. Mouse Leydig cells respond to exogenous stimuli (chorigonadotropin, dibutyryl cyclic AMP) with 2.4-fold higher testosterone secretion than rat cells. A 1.7-fold increased conversion of androgen precursors to testosterone by mouse compared with rat Leydig cells is demonstrated in static incubations as well as in steady-state superfusion experiments and can be derived from enhanced androstenedione reduction and a less inhibitory effect of progesterone on this process is mouse Leydig cells.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 4 (1983), S. 390-392 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: This paper describes a microcomputer-based method for collection and treatment of data from an analytical isotachophoresis apparatus having an array of detectors along the separation trough. The electric field distribution within the separation column is measured as a function of time by means of 256 equidistant detector electrodes. This allows monitoring the detailed approach of the steady isotachophoretic state in a fully automated fashion. Collecting data as well as software for data treatment are discussed together with illustrations.
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